Virtual reality (VR) simulation has been suggested to objectively assess endovascular skills. The aim of this study was to determine the impact of cognitive training on technical performance of inexperienced subjects on a commercially available VR simulator (VIST, Vascular Intervention Simulation Trainer, Mentice, Gothenburg, Sweden).
Methods
Forty-seven subjects treated an identical virtual iliac artery stenosis endovascularly. Surgical trainees without endovascular experience were allocated to two training protocols: group A1 (n = 10) received a 45 minute didactic session followed by an expert demonstration of the procedure that included error-based learning, whereas group A2 (n = 10) was only given a demonstration of an iliac dilation and stent procedure. All trainees performed the intervention immediately following the expert demonstration. Twenty-seven endovascular physicians were recruited (>100 endovascular interventions). Performance was assessed using the quantitative (procedure and fluoroscopy time) and qualitative (stent/vessel ratio and residual stenosis) assessment parameters recorded by the simulator.
Results
The end-product (qualitative metrics) in the cognitive-skills group A1 was similar to those of the endovascular physicians, though A2 performed significantly worse than the physicians (group B): stent/vessel ratio (A1 0.89 vs B 0.96, P = .960; A2 0.66 vs B 0.96, P = .001) and residual stenosis (A1 11 vs B 4%, P = .511; A2 35 vs B 4%, P < .001). Group A1 took longer to perform the procedure (A1 982 vs B 441 seconds, P < .001), with greater use of fluoroscopy than group B (A1 609 vs B 189 seconds, P < .001) whereas group A2 performed the intervention as quickly as group B (A2 358 vs B 441 seconds, P = .192) but used less fluoroscopy (A2 120 vs 189 seconds, P = .002).
Conclusion
Cognitive-skills training significantly improves the quality of end-product on a VR endovascular simulator, and is fundamental prior to assessment of inexperienced subjects.
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The study was funded by Grant support: Funding from the Imperial College Healthcare Biomedical Research Centre, Clinical Doctoral Grant from the Fund for Scientific Research – Flanders, Belgium and from Mentice, Gothenburg, Sweden. Material support: Boston Scientific Corporation.
Competition of interest: none.
Additional material for this article may be found online at www.jvascsurg.org.